FDA Inspection 955220 — Menicon Singapore Pte Ltd
The FDA completed an inspection of Menicon Singapore Pte Ltd on Dec 15, 2015 in Singapore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 15, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Singapore (Singapore)